An essential building block for a successful organization

Since it's inception as "Wells & Associates" in 2000, QualityHub, Inc. has been highly regarded for its high level of expertise. Standing firm on two beliefs; "Always do the right thing!" and "Always strive to make our customers extremely satisfied!", we grew from an organization with one associate to over 30 active associates and a staff of full time employees in 8 years.

Our average consultant regulatory experience is over 27 years. We provide Consulting Associates with expertise in several technical areas: CAPA, Auditing, Management Review, Risk Analysis, Document Control, Sterilization, Process Validation, Software Validation, Performance Scorecard, Part 11, Stability, Process Mapping, Materials, Training, Human Resources, and Laboratories.

We also perform project management and develop Compliance Master Plans for companies facing FDA challenges. We have several consultants who are ex-FDA Investigators and Compliance Officers. We can perform mock-inspections at your facility and assist during FDA inspections. We can review FDA 483s and Warning Letters and other correspondence between you and FDA - making recommendations from ex-FDA and Industry perspectives.

With clients in almost every part of the globe, we are confident we can help your organization with the issues you are facing. Contact us to experience the QualityHub difference.

>> Click here for the QualityHub Corporate Overview: QHub.com Downloads Section